Canonical Allele Identifier: CA2216893876
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094470G= , CM000678.2:g.31094470G= GRCh38
NC_000016.9:g.31105791G= , CM000678.1:g.31105791G= GRCh37
NC_000016.8:g.31013292G= NCBI36
NG_011564.1:g.5486C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.173+87C= MANE Select ENSP00000378426.2:n.173+87C=
ENST00000300851.10:c.173+87C= ENSP00000300851.6:n.173+87C=
ENST00000319788.11:c.173+87C= ENSP00000326135.7:n.173+87C=
ENST00000354895.4:c.173+87C= ENSP00000346969.4:n.173+87C=
ENST00000394971.7:c.32C= ENSP00000378422.3:p.Pro11=
ENST00000394975.2:c.173+87C= ENSP00000378426.2:n.173+87C=
ENST00000420057.2:c.245+919C=
ENST00000498155.1:c.270+919C= ENSP00000417662.1:n.270+919C=
ENST00000529564.1:c.173+87C= ENSP00000431371.1:n.173+87C=
ENST00000532364.1:c.173+87C= ENSP00000460316.1:n.173+87C=
ENST00000533518.5:c.46+87C=
NM_001311311.1:c.173+87C= NP_001298240.1:n.173+87C=
NM_024006.4:c.173+87C= NP_076869.1:n.173+87C=
NM_024006.5:c.173+87C= NP_076869.1:n.173+87C=
NM_206824.1:c.173+87C= NP_996560.1:n.173+87C=
NM_206824.2:c.173+87C= NP_996560.1:n.173+87C=
XM_011545944.1:c.173+87C= XP_011544246.1:n.173+87C=
XM_011545945.1:c.173+87C= XP_011544247.1:n.173+87C=
XR_950848.1:n.961+87C=
NM_024006.6:c.173+87C= MANE Select NP_076869.1:n.173+87C=
NM_001311311.2:c.173+87C= NP_001298240.1:n.173+87C=
NM_206824.3:c.173+87C= NP_996560.1:n.173+87C=